Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13282생성일: 2026년 10월 24일
Iodoacetamide → 2-(2-(6-(4-Fluoro-phenoxy)-2-pyridin-2-yl-3H-benzimidazol-5-yl)-pyrrolidin-1-yl)-acetamide
https://huagongshe.com/ko/reaction/13282
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Iodoacetamide | HCID 3727 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 5-(4-fluoro-phenoxy)-2-pyridin-2-yl-6-pyrrolidin-2-yl-1H-benzimidazole | HCID 23145575 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 2-(2-(6-(4-Fluoro-phenoxy)-2-pyridin-2-yl-3H-benzimidazol-5-yl)-pyrrolidin-1-yl)-acetamide | HCID 23145124 | — |
반응 단계
11.4 mg of potassium carbonate and 11.1 mg of iodoacetamide were added in order to an acetonitrile (1 ml) solution of 20 mg of 5-(4-fluoro-phenoxy)-2-pyridin-2-yl-6-pyrrolidin-2-yl-1H-benzimidazole obtained in Example 168, and the reaction liquid was stirred overnight at room temperature. The reaction liquid was concentrated, and the resulting residue was purified through reversed-phase middle-pressure liquid chromatography [ODS-AS-360-CC (by YMC), mobile phase: water-acetonitrile-0.1% trifluoroacetic acid], and the resulting fraction was diluted with ethyl acetate, washed with aqueous saturated sodium bicarbonate and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain the entitled compound as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07728025B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-82f3e1f2420e4be1992565f49031ff26 |
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| 출처 메모 | uspto-grants-2010_06 |
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